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Effects of liraglutide and sibutramine on food intake, palatability, body weight and glucose tolerance in the gubra DIO-rats.

AbstractAIM:
To validate the gubra DIO-rats as a useful animal model of human obesity.
METHODS:
The gubra diet-induced obesity (DIO) rat model was based on male Sprague-Dawley rats with ad libitum access to regular chow and a palatable diet rich in fat and sugar. To evaluate the versatility of the gubra DIO-rats as a valid model of human obesity syndrome, the efficacy of 2 weight loss compounds liraglutide and sibutramine with different mechanisms of action were examined in 7-month-old gubra DIO-rats. Liraglutide (200 μg/kg, sc) was administered bi-daily, and sibutramine (5 mg/kg, po) was administered once daily for 23 d.
RESULTS:
Both the compounds effectively reduced the food intake, body weight and total fat mass as measured by nuclear magnetic resonance. Whereas the 5-HT reuptake inhibitor/5-HT receptor agonist sibutramine reduced the intake of both chow and the gubra-diet, the GLP-1 analogue liraglutide predominantly reduced the intake of the highly palatable diet, indicating a shift in food preference. Sibutramine lowered the insulin sensitivity index, primarily via reductions in glucose-stimulated insulin secretion.
CONCLUSION:
This animal model responds well to 2 weight loss compounds with different mechanisms of action. Moreover, the gubra DIO-rat can be particularly useful for the testing of compounds with potential effects on diet preference.
AuthorsGitte Hansen, Jacob Jelsing, Niels Vrang
JournalActa pharmacologica Sinica (Acta Pharmacol Sin) Vol. 33 Issue 2 Pg. 194-200 (Feb 2012) ISSN: 1745-7254 [Electronic] United States
PMID22301859 (Publication Type: Journal Article)
Chemical References
  • Anti-Obesity Agents
  • Cyclobutanes
  • Liraglutide
  • Glucagon-Like Peptide 1
  • sibutramine
Topics
  • Animals
  • Anti-Obesity Agents (pharmacology, therapeutic use)
  • Body Weight (drug effects)
  • Cyclobutanes (pharmacology, therapeutic use)
  • Eating (drug effects)
  • Glucagon-Like Peptide 1 (analogs & derivatives, pharmacology, therapeutic use)
  • Glucose Tolerance Test
  • Insulin Resistance
  • Liraglutide
  • Male
  • Obesity (drug therapy)
  • Rats
  • Rats, Sprague-Dawley

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